Isabelle Raingeard
University of Montpellier
44 Papers
106 Citations
Isabelle Raingeard is an academic researcher from University of Montpellier. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 14, co-authored 35 publications.
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Papers
Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis
Thomas Cuny,Morgane Pertuit,M Sahnoun-Fathallah,Adrian Daly,Gianluca Occhi,Marie Françoise Odou,Antoine Tabarin,Marie Laure Nunes,Brigitte Delemer,Vincent Rohmer,Rachel Desailloud,Véronique Kerlan,Olivier Chabre,Jean-Louis Sadoul,M. Cogne,Philippe Caron,Christine Cortet-Rudelli,Anne Lienhardt,Isabelle Raingeard,Anne-Marie Guedj,Thierry Brue,Albert Beckers,Georges Weryha,Alain Enjalbert,Anne Barlier +24 more
TL;DR: Mutations in MEN1 can be of significance in young patients with sporadic isolated pituitary macroadenomas, particularly PRL, and together with AIP, are suggested to suggest genetic analysis of MEN1 in such a population.
Steroidogenic factor-1 (SF-1) gene mutation as a frequent cause of primary amenorrhea in 46,XY female adolescents with low testosterone concentration
Pascal Philibert,Elodie Leprieur,Delphine Zenaty,Elisabeth Thibaud,Michel Polak,Anne-Marie Frances,James Lespinasse,Isabelle Raingeard,Nadège Servant,Françoise Audran,Françoise Paris,Charles Sultan +11 more
TL;DR: The genetic analysis of low-testosterone primary amenorrhea is complex as several factors may be involved, and underlines the need to systematically analyze the SF1 sequence in girls with primary Amenorrhea due to 46, XY DSD and low testosterone, as well as in newborns with 46,XY DSD.
Optimizing the outcome of pregnancy in obese women: from pregestational to long-term management.
TL;DR: Optimal management includes preconception counselling, pregravid weight-loss programmes, monitoring of gestational weight gain, repeated screening for pregnancy complications and long-term follow-up to minimize the social and economic consequences of pregnancy in overweight women.
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Global Sequencing Approach for Characterizing the Molecular Background of Hereditary Iron Disorders
Séverine Cunat,Muriel Giansily-Blaizot,Michael Bismuth,François Blanc,Olivier Dereure,Dominique Larrey,Alain Le Quellec,Philippe Pouderoux,Christian Rose,Isabelle Raingeard,Eric Renard,Jean-François Schved,Patricia Aguilar-Martinez +12 more
TL;DR: A rapid automated method for sequencing the main genes involved in hereditary iron overload or HF and allows rapid evaluation of patients is developed.
Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) on diagnosis of Cushing's syndrome.
Antoine Tabarin,Guillaume Assié,Pascal Barat,Fidéline Bonnet,Jean-François Bonneville,Françoise Borson-Chazot,Jérôme Bouligand,A. Boulin,Thierry Brue,Philippe Caron,Frederic Castinetti,Olivier Chabre,Philippe Chanson,Jean-Benoît Corcuff,C. Cortet,Régis Coutant,Anthony Dohan,Delphine Drui,Stéphanie Espiard,Delphine Gaye,Solenge Grunenwald,Laurence Guignat,Elif Hindié,Frédéric Illouz,Peter Kamenicky,Hervé Lefebvre,Agnès Linglart,Laetitia Martinerie,Marie-Odile North,Marie Laure Raffin-Samson,Isabelle Raingeard,Gérald Raverot,Véronique Raverot,Yves Reznik,David Taieb,Delphine Vezzosi,Jacques Young,Jérôme Bertherat +37 more
TL;DR: In this paper , the authors present a consensus paper by 38 experts of the French Society of Endocrinology and the French society of Pediatric Endocrine and Diabetology aimed firstly to detail the circumstances suggesting diagnosis and the biologic diagnosis tools and their interpretation for positive diagnosis and for etiologic diagnosis according to ACTH-independent and -dependent mechanisms.